Canonical Allele Identifier: PA313546
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 205014
ClinVar RCV Id: RCV000186925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Trp182Arg
CA313545
NM_000744.7:c.544T>C
CA409638055
NM_000744.7:c.544T>A